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NCT06582810 · ClinicalTrials.gov registry record

Lidocaine Infusion Treatment for Subarachnoid Hemorrhage Headaches

A clinical trial of Headache and Subarachnoid; Hemorrhage, Nontraumatic, sponsored by University of Kansas Medical Center.

Recruiting
Registry status
20
Enrollment target
1
Study location

NCT06582810 is a study of Headache and Subarachnoid; Hemorrhage, Nontraumatic that is actively recruiting participants, run by University of Kansas Medical Center. The registered enrollment target is 20 participants, below the 155-participant average among 35 other Headache trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06582810, a study of Headache and Subarachnoid; Hemorrhage, Nontraumatic, is actively recruiting participants, sponsored by University of Kansas Medical Center.

RECRUITING
Registry status
20 participants
Enrollment target
1
Study location

Study Summary

The goal of this observational study is to evaluate intravenous lidocaine efficacy and safety in treating headache following non-traumatic subarachnoid hemorrhage. Through this prospective analysis, the investigators hope to: 1. show that intravenous lidocaine infusion causes a clinically significant reduction in pain scores in patients with moderate/severe headache pain following non-traumatic subarachnoid hemorrhage; 2. show that intravenous lidocaine infusion is safe in treating headache following non-traumatic subarachnoid hemorrhage; 3. and report vasospasm prevalence in the cohort. Participants will receive lidocaine infusion as treatment for non-traumatic subarachnoid hemorrhage headache and provide pain scores (on a numeric pain scale) every two hours the patients are awake for a maximum of seven days. Monitoring for vasospasm will occur as part of the patients regular medical care.

Study Locations (1)

Kansas

  • Ascension Via Christi St. Francis - Wichita

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2025-01-31
Est. Completion 2028-07

Sponsor

University of Kansas Medical Center

408 total trials

What the Registry Record Tells You About NCT06582810

The ClinicalTrials.gov registry entry for NCT06582810 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 155-participant average among 35 other Headache trials with a reported enrollment target (87% lower). The listed sponsor is University of Kansas Medical Center, which has 408 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Headache appearing as the primary indexed condition, and to 0 interventions.

NCT06582810 reports 1 study location spanning 1 distinct geographic area - top geographies include Kansas.

Frequently Asked Questions

What is clinical trial NCT06582810 about?

NCT06582810 is a clinical study titled "Lidocaine Infusion Treatment for Subarachnoid Hemorrhage Headaches". The goal of this observational study is to evaluate intravenous lidocaine efficacy and safety in treating headache following non-traumatic subarachnoid hemorrhage. Through this prospective analysis, the investigators hope to: 1. show that intravenous lidocaine infusion causes a clinically significa...

What is the current status of trial NCT06582810?

This trial is currently recruiting. The enrollment target is 20 participants. The study started on 2025-01-31. Estimated completion is 2028-07.

What conditions does trial NCT06582810 study?

This clinical trial studies the following conditions: Headache, Subarachnoid; Hemorrhage, Nontraumatic.

Who is sponsoring clinical trial NCT06582810?

This trial is sponsored by University of Kansas Medical Center, which has 408 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06582810 being conducted?

This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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